Senior Statistician

About the role

Worldwide Clinical Trials is seeking a Senior Statistician to independently manage statistical project support and provide expert consultancy across its global CRO operations.

Key responsibilities

• Manage statistical support for one or more clinical trial projects, ensuring timely expert consultancy.
• Review study designs, analysis plans, and reports, and assist sponsors with protocol and randomization methodology.
• Develop, evaluate, and run SAS programs for CDISC SDTM and ADaM datasets, tables, figures, and listings.
• Produce final reports, including tables, listings, figures, and manuscript contributions.
• Support bidding processes, budget reviews, and proposal development.
• Lead system and process improvements to enhance data processing efficiency.

Required profile

• Master's degree in mathematics, statistics, or a related quantitative field.
• Minimum 3 years of statistical experience leading clinical trial projects and data analysis.
• Expert-level project statistician with strong customer focus and communication skills.

Required skills

• Proficiency in SAS programming.
• Experience with CDISC standards (SDTM, ADaM).
• Knowledge of nQuery for sample size calculations.
• Familiarity with ICH, FDA, and CPMP regulatory guidance.